Teva Pharmaceuticals recalls Granix (tbo-filgrastim) injection due to stability test failure. This may affect medication safety. Check product details to see if you have recalled items.
Failed Stability Specifications - 12-month stability test result for one of the known peptides is below the specification limit
Teva Pharmaceuticals is recalling Granix (tbo-filgrastim) injections because a stability test showed one of the key peptides didn't meet quality standards. This could mean the medication might not work properly or be unsafe for patients who need it.
The stability test for one of the key peptides in the medication fell below the required safety limits. This could mean the medication might not be effective or could pose a safety risk if stored or used incorrectly.
Patients using Granix injections for cancer treatment or immune support are likely affected. Those with the specific product lot numbers and expiration dates listed in the recall are at most risk.
Check for Granix injections with NDC codes 63459-910-11, 63459-910-15, or 63459-910-17. Look for lot numbers 135738, 137149, or 137148 and expiration date 09/30/2025.
Identify if your Granix injection has the NDC codes and lot numbers listed in the recall.
The recall states the product failed a stability test, but it does not specify that the product is unsafe to use. Patients should check if they have the recalled items and follow the action steps.
The recall does not provide a remedy, so you should check the product details to see if it matches the recalled items and contact Teva Pharmaceuticals for further instructions.
Check the NDC codes and lot numbers listed in the recall: NDC 63459-910-11, 63459-910-15, 63459-910-17 with lot numbers 135738, 137149, or 137148 and expiration date 09/30/2025.
We’ve drafted a message you can send Teva to request your refund or repair — edit it as you like.
Subject: Recall D-0218-2025 — Teva Teva Hello, I own a Teva that is covered by recall D-0218-2025 from Teva. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
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The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
